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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411528Generated: October 26, 2026

Water → 4-[1-(3,4-Dimethoxyphenoxy)-4-hydroxybutyl]benzonitrile

https://huagongshe.com/reaction/411528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
Reactant4-[1-(3,4-Dimethoxyphenoxy)-3-butenyl]benzonitrileHCID 21867689—
ReactantSodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
SolventTetrahydrofuranHCID 8028—
Product4-[1-(3,4-Dimethoxyphenoxy)-4-hydroxybutyl]benzonitrileHCID 2186772678%

Reaction Steps

Borane-methyl sulfide complex (2 M in ether, 11 mL, 22 mmol) was added dropwise to a cooled (−5° C.) solution of 4-[1-(3,4-dimethoxyphenoxy)-3-butenyl]benzonitrile (see step (i) above; 17.6 g, 56.8 mmol) in dry THF (15 mL) over a period of 15 minutes (during which time the reaction temperature rose to 0° C.). The resulting mixture was stirred at between 0 and 10° C. for 1.5 h, before being allowed to warm to rt. Stirring was continued for a further 3.5 h at this temperature before water (22 mL) and sodium perborate tetrahydrate (11 g, 66 mmol) were added. The biphasic mixture was stirred for 2 h at rt before the water layer was separated and extracted with ether. The combined organic layers were washed with brine, dried and concentrated in vacuo. The resulting residue was purified by chromatography on silica gel, eluting with IPA: ethyl acetate:heptane (5:25:70) to yield 14.5 g (77%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559162B2
Source datasetuspto-grants-2003_05
ORD IDord-905cf7aef2f244178ccf9ab56e404455
Source noteuspto-grants-2003_05